introduction to tddft - institut...
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Introduction to TDDFTLinear-Response TDDFT
in Frequency-Reciprocal spaceon a Plane-Waves basis:
the DP (Dielectric Properties) code
Valerio Olevano
Institut Néel, CNRS, GrenobleEuropean Theoretical Spectroscopy Facility
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Résumé
• Motivation• TDDFT• Linear-Response TDDFT• Frequency-Reciprocal space TDDFT• TDDFT on a PlaneWaves basis: the DP
code• Approximations: RPA, ALDA, new kernels• Results• Conclusions
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Condensed Matter Theories• Models:
– Jellium– Anderson– Hubbard -> DMFT
• Semi-Empirical and Phenomenological Theories:– Tight Binding– ...
• Ab Initio First-Principles or Microscopical Theories:– CI– QMC– DFT, TDDFT– MBPT (GW and Bethe-Salpeter Equation)
analytic(but C-DMFT medium numerical)
lightly numerical
heavy numerical
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What DFT can predict(normal error 1~2% in the 99% of cond-mat systems)
• Atomic Structure, Lattice Parameters (XRD)
• Total Energy, Phase Stability• Electronic Density (STM, STS)• Elastic Constants • Phonon Frequencies (IR, Neutron scattering, Raman)
that is, all Ground State Properties!
DFT-LDA nlcc DFT-LDA semic EXP [Longo et al.]ab 4.641 Å 4.522 Åc 5.420 Åα 121.46
5.659 Å 5.549 Å 5.7517 ± 0.0030 Å4.5378 ± 0.0025 Å
5.303 Å 5.3825 ± 0.0025 Å121.73˚ 122.646˚ ± 0.096
Vanadium Oxide, VO2
latticeparametersM. Gatti et al., PRL accepted
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What DFT cannot predict
• Electronic Structure, Bandplot• Bandgap, Metal/Insulator/Semiconductor• Optical and Dielectric propertiesthat is, all Excited State Properties!
You may use DFT to predict all such propertiesbut it cannot be blamed if it does not succeed.
F. Bruneval et al., PRL 2006
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Lautenschlager et al. PRB 36, 4821 (1987).
Aspnes and StudnaPRB 27, 985 (1983).
Aspnes and StudnaPRB 27, 985 (1983).
Reflectance
Optical AbsorptionRefraction Index
Optical Spectroscopies
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Stiebling Z. Phys. B 31, 355 (1978).
Energy Loss (EELS)
Energy-Loss Spectroscopies
Sturm et al.PRL 48, 1425 (1982),(ESRF, Grenoble)
Schuelke and KaprolatPRL 67, 879 (1991)(ESRF, Grenoble).
Coherent InelasticScattering Spectroscopy (CIXS)
Inelastic X-ray ScatteringSpectroscopy (IXSS)
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Why we need ab initio theoriesto calculate spectra
1)To understand and explain observed phenomena2)To offer experimentalists reference spectra3)To predict properties before the synthesis, the
experiment
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Excitations: Charged vs Neutral
Inverse Photoemission Optical Absorption
c
v
c
v
e hν
hν
Charged ExcitationsN -> N+1 (or N-1)
(Photoemission Spectroscopy)
Neutral ExcitationsN -> N
(Optical and DielectricSpectroscopy)
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Excitations: Charged vs Neutral
Inverse Photoemission Optical Absorption
electron-electroninteraction +
electron-hole interaction
c
v
c
v
electron-electroninteraction
Charged ExcitationsN -> N+1 (or N-1)
Neutral ExcitationsN -> N
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Photoemission Spectroscopy
direct photoemission
sample
e-
hν
inverse photoemission
sample
hν
e-
c
v
hν
e-
c
v
hν
e-
LURE Orsay, Sirotti et al.
dete
ctor
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Optical Spectroscopy
incidentphoton
reflectedphoton
transmittedphoton
sample
hν
detector
Valerio Olevano, Introduction to TDDFT
c
v
ωcv
hν
Cardona et al.
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Dielectric, Energy-Loss Spectroscopy (EELS)
c
v
ωcv
e-
e-
c
v ωp
e-
plasmon
e-
sample
e-
e-
electrons
detector
Lautenschlager
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Synchrotron Radiation Spectroscopy (IXSS)
c
v
ωcv
c
v ωp
plasmon
ESRF, Grenoble
X
sample
X rays
detector
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Possible ab-initio Theoriesfor the Excited States
• TDDFT (Time-Dependent Density-Functional Theory) in the Approximations:– RPA– TDLDA– beyond
• MBPT (Many-Body Theory) in the Approximations:– GW– BSE (Bethe-Salpeter Equation approach)
Charged Excitations
NeutralExcitations
NeutralExcitations
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What is TDDFT?
• TDDFT is an extension of DFT; it is a DFT with time-dependent external potential:
v r ⇔r
v r ,t ⇔r , t
Hohenberg-Kohntheorem
Runge-Grosstheorem
• Fundamental degree of freedom: Time-Dependent electronic Density ρ(r,t) (instead of the total many-body wavefunction Ψ(r
1,...,r
N,t))
Valerio Olevano, Introduction to TDDFT
Static Ionic Potential
Static Ionic Potential+
External Perturbation(E.M. field)
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TDDFT milestones
• Runge and Gross (1984): rigorous basis of TDDFT.
• Gross and Kohn (1985): TDDFT in Linear Response.
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The Runge Gross theorem
i∂t1t= T V 1t W 1t
i∂t2t = T V 2t W 2 t
v1t≠v2t c t ⇒ 1t ≠2t
ot=⟨t∣o∣t⟩=o[]t
Any observable is functionalof the (time-dependent) density:
ρ(t)
t
ρ1
ρ2
v1
v2
PRL 52, 997 (1984)
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Runge Gross theorem caveats
ot=o [ ,0] t 1) Any observable is functional of the density
and of the initial state Ψ0=Ψ(t
0)
2) The Runge-Gross theorem has been proven for v(t) Taylor expandable around t
0. And if you run into problems
already in describing the (nonequilibrium) initial state, you can't go on with TDDFT. Previous demonstrations required periodic v(t) or a small td perturbation (linear response), or later (Laplace transformable switch-on potentials+initial ground-state). But there is no very general prove of the Runge Gross theorem.
t
v(t)
t0
What about this case?
t
v(t)
t0
This other is also notRunge-Gross described
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TDDFT vs DFTZoological Comparative Anatomy
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DFT vs TDDFTHohenberg-Kohn: Runge-Gross:
The Total Energy: The Action:
are unique functionals of the density.
The stationary points of the:
Total Energy Action
give the exact density of the system:
∫t0
t1
dt ⟨t ∣i∂t−H t ∣t⟩=A[]⟨∣ H∣⟩=E []
E [] r
=0
r ,t
A[] r ,t
=0
r
v r ,t ⇔r , tv r ⇔r
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The extrema of the:
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DFT vs TDDFTKohn-Sham: Runge-Gross:
Kohn-Sham equationsi∂ti
KSr ,t =HKS
r , tiKSr , tHKS
r iKSr =i
KSi
KSr
r ,t =∑i=1
N
∣iKSr ,t∣
2r =∑
i=1
N
∣iKSr ∣
2
vKSr , t=v r , t∫dr 'r ' ,t ∣r−r '∣
Axc[ ]
r , tvKSr =v r ∫dr '
r '∣r−r '∣
Exc []
r
Valerio Olevano, Introduction to TDDFT
ρ(t)
t
ρv
ρ(t)
t
ρvKS
W W=0
real system Kohn-Sham system
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TDDFT further caveats1) The functional A
xc[ρ] is defined only for v-
representable densities. It is undefined for ρ which do not correspond to some potential v -> problems when variations δA[ρ] with respect to arbitrary densities are required in order to search for stationary points.
2) A functional A[ρ] with ρ(t) on the real time, is hill defined, since we would run in a causality-symmetry paradox -> we can solve the problem by declaring t on the Keldysh contour. Response functions are symmetric on the contour and become causal on physical time.
A[] r ,t
=0 Axc [ ]
r ,t
A v r , t v r 't '
= r ,t v r ' t '
symmetric causal (=0 for t'>t)
As []
r ,t =vsr ,t
A[v ]=−A[]∫dr dtr ,t v r , t
A[v ] v r , t
=r , t
If exists
Then we can define theLagrange transform:
t0 t
Van Leeuwen, PRL 80, 1280 (1998).
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TDDFT in Linear Response Gross and Kohn (1985)
• If:
TDDFT = DFT + Linear Response(to the time-dependent perturbation)
• with:
v r ,t =v r v r , t
v r ,t ≪v r
Valerio Olevano, Introduction to TDDFT
Strong (Laser) perturbations excluded!
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Hohenberg-Kohn Theorem for Linear Response TDDFT
v r ⇔r
v r ,t ⇔r , t
v r v r , t⇔r r , t
v r ,t ⇔r ,t
DFT:
TDDFT:
LR-TDDFT:
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Calculation Scheme
DFT calculation (ABINIT code)
LR-TDDFT calculation (DP code)
v r ⇒r ,iKS ,i
KS
v r ,t ⇒ r ,t ,
v, spectra
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Polarizability χ
External Perturbation(variation in the external potential)
Polarizability χ
implicit definition of the polarizability χ:
vext
= vext
Induced Density(variation in the density induced by δv
ext)
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Variation in the Total Potential
The variation in the density induces a variation in the Hartreeand in the exchange-correlation potentials which screen the external perturbation:
vH= vH
=v c
vtot=vext vHv xc
So that the variation in the total potential (external + screening) is:
v xc=vxc
= f xc
Total Perturbation
f xc=vxc
Exchange-CorrelationKernel definition
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LR-TDDFT Kohn-Sham scheme:the Independent Particle Polarizability χ(0)
Let's introduce a ficticious s, Kohn-Sham non-interacting system such that:
Independent ParticlePolarizability χ (0)=
0 vtot
s=
Then, instead of calculating χ, we can more easily calculate the polarizability χ(0) (also χ
s or χKS) of this non-interacting system,
called independent-particle polarizability and defined:
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the Independent Particle Polarizability χ(0)
Independent-Particle Polarizability (Adler-Wiser)0r ,r ' ,=∑ij
f i− f jir * jr *i r ' jr '
−i− j−i
By variation δvtot
(= δvs = δvKS) of the Kohn-Sham equations, one obtains the
Linear-Response variation of the density δρ and then an expression for χ(0
in terms of the Kohn-Sham energies and wavefunctions:
GG'0 q ,=∑ij
f i− f j⟨ j∣e
−i qGr∣i⟩ ⟨i∣e
i qG'r∣ j⟩
−i− j−i
In Frequency-Reciprocal space:
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χ as a function of χ(0)
Polarizability χ
Exchange-Correlation KernelCoulombian (Local-Fields)
=0
0vc f xc
=1−0vc−0 f xc
−10
Also explicitly:
The polarizability in terms of the independent-particle polarizability is:
= vext
=0vtot
From:
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Dielectric Function
definition of the Dielectric Function ε
Test-ParticleDielectric Function
−1=1vc
vtot=−1vext
te−1=1vc f xc Test-Electron Dielectric Function
GG'−1q , In a periodic system
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Macroscopic Dielectric Function
MacroscopicDielectric Function ε
Μ
M q ,=1
00−1q ,
Observables
Macroscopic Dielectric Function εΜ
ABS=ℑMEELS=−ℑM
−1
M r ,r '=r ,r '
MLF≠00=M
NLF
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TDDFT: fundamental equations
χ (0)(r, r', ) ( fi f j)i (r) j
* (r) i*(r') j(r')
i ε j ω − ii j
Dielectric Function ε
Polarizability χ
Independent-Particle Polarizability (Adler-Wiser)
Exchange-Correlation Kernel
Exchange-Correlation KernelCoulombian (Local-Fields)
ObservablesABS = Im ε
EELS = -Im ε−1
=0
0vc f xc
−1=1vc
f xc= vxc
=?
approximations required
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Local-Fields Effects (LF)
Macroscopic Dielectric Function ε without local-fields effects (NLF)
vGtot=∑
G 'GG'−1 vG '
ext Effect of the ε non diagonal elements (density inhomogeneities)
MNLFq ,=00 q ,
vext−1~ vtot
+ →
Valerio Olevano, Introduction to TDDFT
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LR-TDDFT Calculation SchemeRésumé
DFT
KSDFT
KSDFT
f xc0
MValerio Olevano, Introduction to TDDFT
![Page 37: Introduction to TDDFT - Institut Néelperso.neel.cnrs.fr/valerio.olevano/resint/tddft/tddft.pdfIntroduction to TDDFT Linear-Response TDDFT in Frequency-Reciprocal space on a Plane-Waves](https://reader030.vdocuments.site/reader030/viewer/2022040905/5e799ff43823e54adf3be88c/html5/thumbnails/37.jpg)
dp code(dielectric properties)
• The thing: Linear-Response TDDFT code in Frequency-Reciprocal Space on PWbasis.
• Purpose: Dielectric and Optical Properties (Absorption, Reflectivity, Refraction, EELS, IXSS, CIXS,..
• Systems: bulk, surfaces, clusters, molecules, atoms (through supercells) made of insulator, semiconductor and metal elements.
• Approximations: RPA, ALDA, GW-RPA, LRC, non-local kernels, …, with and without LF (Local Fields).
• Machines: Linux, Compaq, IBM, SG, Nec (6GFlop) , Fujitsu.• Libraries: BLAS, Lapack, CXML, ESSL, IMSL, ASL, Goedecker, FFTW.• Interfaces: ABINIT, Milan-CP, PWSCF, SPHINGx
http://www.dp-code.org
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Frequency-Reciprocal space:why and where could be convenient
• Reciprocal Space -> Infinite Periodic Systems (Bulk, but also Surfaces, Wires, Tubes with the use of Supercells);
• Frequency Space -> Spectra.
Valerio Olevano, Introduction to TDDFT
In the case of isolated systems (atoms, molecules) it is more convenienta real space-time approach (e.g. Octopus code)
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DP Flow Diagrami
KSGi
KS
f xc
GG'0 q ,=∑ij
f i− f jijG *ij G'
i− j−
GG' q ,
GG'−1q ,
MLFq ,
iKSr
ijr =*ir jr
ijG
MNLFq ,
FFT-1
FFT
INV
DFT-code interface
![Page 40: Introduction to TDDFT - Institut Néelperso.neel.cnrs.fr/valerio.olevano/resint/tddft/tddft.pdfIntroduction to TDDFT Linear-Response TDDFT in Frequency-Reciprocal space on a Plane-Waves](https://reader030.vdocuments.site/reader030/viewer/2022040905/5e799ff43823e54adf3be88c/html5/thumbnails/40.jpg)
DP tricks
GG'=1−0vc−
0 f xcGG' '−1
G''G'0
we solve the linear system for only the first column of
If we only need that is only then instead of solving (inverting a full matrix):
1−0v c−0 f xc GG'G'0=G 0
0
0000−1=1−v000
G'0
O(N2) instead of O(N3)
![Page 41: Introduction to TDDFT - Institut Néelperso.neel.cnrs.fr/valerio.olevano/resint/tddft/tddft.pdfIntroduction to TDDFT Linear-Response TDDFT in Frequency-Reciprocal space on a Plane-Waves](https://reader030.vdocuments.site/reader030/viewer/2022040905/5e799ff43823e54adf3be88c/html5/thumbnails/41.jpg)
DP Parametersi
KSGi
KS
f xc
GG'0 q ,=∑ij
f i− f jijG *ij G'
i− j−
GG' q ,
GG'−1q ,
MLFq ,
iKSr
ijr =*ir jr
ijG
MNLFq ,
FFT-1
FFT
INV
NG = npwwfn
Nb = nbands
NG = npwmat
Nω = nomega
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DP performances:CPU scaling and Memory usage
• CPU scaling for• CPU scaling for• Memory occupation
0 : N bN kNNG
2N r logN r
−1 : NNG
2
NNG2Nr N kN b
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Exchange-Correlation Kernel fxc
:
the RPA approximation
• Random Phase Approximation = neglect of the exchange-correlation effects (in the response)
– RPA f xc
RPA=0
![Page 44: Introduction to TDDFT - Institut Néelperso.neel.cnrs.fr/valerio.olevano/resint/tddft/tddft.pdfIntroduction to TDDFT Linear-Response TDDFT in Frequency-Reciprocal space on a Plane-Waves](https://reader030.vdocuments.site/reader030/viewer/2022040905/5e799ff43823e54adf3be88c/html5/thumbnails/44.jpg)
RPA ApproximationRPA (without Local Fields) = sum over independent transitions (application of Fermi’s Golden Rule to an independent particle system)
Fermi’s Golden Rule
KS energies
Optical Absorption
KS wavefunctions
c
v
ωcvhν
solidf
i
ωfihν
confined system
ℑRPA =∑vc∣⟨c∣
D∣v ⟩∣2−c−v
Valerio Olevano, Introduction to TDDFT
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Adiabatic Local Density Approximation (TDLDA)
• The Adiabatic Local Density Approximation
– ALDAf xc
ALDA=v xc
LDA
=0
f xcALDA
r ,r '=Ar r ,r ' local in r-spaceno memory effect
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TDDFT: Results
no noOptical Prop
ok okEnergy Loss
Solids
ok but.. ok but..Optical Prop
ok okEnergy Loss
Isolated
ALDARPA
Energy Loss -> -Im ε-1
Optical Properties -> Im ε
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TDDFT: Results
Energy Loss
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TDDFT and EELS in Solids
• TDLDA (but also RPA) in good agreement with experiment;
• Importance of Local-Field (LF) effects.
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Local Field Effects in EELS
• RPA is enough. But when inhomogeneities are present, Local-Field effects should be absolutely taken into account.
• Quantitative Agreement
A. Marinopoulos et al. PRL 89, 76402 (2002)
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IXSS and CIXSand other synchrotron-radiation spectroscopies
• In Solids all Dielectric Properties related to the Energy-Loss function are well described by TDDFT in RPA with an improvement in ALDA.
Weissker et al.
V. Olevano, thesis
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IXSS synchrotron-radiation spectroscopy
• In Solids all Dielectric Properties related to the Energy-Loss function are well described by TDDFT in RPA with an improvement in ALDA.
Weissker et al.
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TDDFT: Results
Optical Properties
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TDDFT RPAOptical Properties in Nanotubes
• RPA is qualitatively able to interpret observed structures in optical spectra
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LF Effects in in C and BN Nanotubes
• LF explain depolarization effects both for C and BN Nanotubes in perpendicular polarization optical spectra
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Optical Absorption in Clusters
G. Onida et al, Rev. Mod. Phys. 74, 601 (2002).
RPA NLFEXP TDLDA
RPA LF
• Fair agreement (improvable) of the TDLDA result with the Experiment.
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Optical Properties in Solids: Si
• The TDLDA cannot reproduce Optical Properties in Solids.
• We miss both:
1 Self-Energy (electron-electron) effects (red shift of the entire spectrum)
2 Excitonic (electron-hole) effects (underestimation of the low-energy part)
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GW: optical properties in Solids
• GW corrects the red-shift but still misses the Excitonic Effects
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MBPT: GW, BSE and Excitonic Effects
P = + + O(2)+
RPA GW BSE
Polarization
e-
h+
c
v
ωcvhν
c
v
ωcvhν
c
v
ωcvhν W
exciton
Valerio Olevano, CNRS, Intoduction to TDDFT
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Bethe-Salpeter Equation: optical properties in Solids
• Almost quantitative agreement of BSE with the experiment
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Solid Argon: Hydrogen series
• Exciton ~ Hydrogen atom → En ~1/n2 Balmer-like series
• BSE can reproduce even bound Excitons
n=1
n=2n=3
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What can we do to solvethe TDDFT kernel problem?
• If a new Approximation in TDDFT could be established, combining TDDFT’s simplicity with MBPT’s reliability…
• Hints for this new Approximation: compare critically MBPT with TDDFT fundamental equations.
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New Approximations:
LRC(Long Range Contribution only)
Nanoquanta kernel(or mapping BSE on TDDFT)
![Page 63: Introduction to TDDFT - Institut Néelperso.neel.cnrs.fr/valerio.olevano/resint/tddft/tddft.pdfIntroduction to TDDFT Linear-Response TDDFT in Frequency-Reciprocal space on a Plane-Waves](https://reader030.vdocuments.site/reader030/viewer/2022040905/5e799ff43823e54adf3be88c/html5/thumbnails/63.jpg)
LRC Approximation
Long Range Contribution onlyf xcLRC=limq0 f xc
MT=−
qG2
=4.6 ∞−1 Inversely proportional to the screening
=0
0vc f xc
long-range coulombian
ALDA: local kernel
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TDDFT, LRC approximation
• The LRC approximation makes TDDFT work also on Optical Properties in Solids
![Page 65: Introduction to TDDFT - Institut Néelperso.neel.cnrs.fr/valerio.olevano/resint/tddft/tddft.pdfIntroduction to TDDFT Linear-Response TDDFT in Frequency-Reciprocal space on a Plane-Waves](https://reader030.vdocuments.site/reader030/viewer/2022040905/5e799ff43823e54adf3be88c/html5/thumbnails/65.jpg)
Nanoquanta kernel
G
Wχ
0
-1
L. Reining, V. Olevano, A. Rubio and G. Onida, (2001)
F. Sottile, V. Olevano and L. Reining, (2004)
A. Marini, R. Del Sole, A. Rubio, (2004)
G. Adragna and R. Del Sole, (2001)
U. Von Barth, N. E. Dahlen, R. Van Leeuwen and G. Stefanucci, (2006)
R. Stubner, I. Tokatly and O. Pankratov, (2006)
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TDDFT vs BSE
4-pointTDDFT
BSE
4-pointCoulombian
KGW = Self-Energy correction diagonal term
TDDFT-BSE Differences:
FTDDFTx1 , x2 , x3 , x4=x1 , x2x3 , x4 f xc x1 , x3
FBSEx1 , x2 , x3 , x4=−x1 , x3x2 , x4 f xcx1 , x2
P x1 , x2 , x3 , x4=0x1, x2, x3, x4
0vcFTDDFT
P
P x1 , x2 , x3 , x4=P 0x1, x2 , x3 , x4P
0 v cFBSE
P
P 0=
0
0KGW P 0
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Nanoquanta fxc
Where:
Kohn-Sham bilinear
GW shift term
Excitonicterm
WARNING: fxc could not exist due to invertibility problems of Φ!
static
PRL 88, 066404 (2002).
f xc q ,G ,G'=∑n1n2n3n4
1 f n1
− f n2−1n1 ,n2 ;GK n1n2 n3n4
*−1n3 ,n4 ;G '
n1 ,n2 ;r =n1r n2
Hr
Kn1n2n3n4=n2
GW−n1
GWn1n3
n2n4 f n1
− f n2F n1n2 n3n4
BSE
Fn1n2n3n4BSE
=−∫dr dr 'n1 ,n3 ; r W r ' ,r * n2 ,n4 ;r '
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Solid Argon: Bound Excitons
• The Nanoquanta kernel makes TDDFT reproduce even Bound Excitons
n=2
n=1
n=3
F. Sottile et al.
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TDDFT Excitation Energiesand the Casida Equations
∑t 'tt ' at '=
2at
tt'=t2tt '2tt ' f tt'
Hxc
t=c−v
f tt 'Hxc=∫dr1dr 2*c r 1v r1[vc r 1 ,r 2 f xc r1 ,r 2 ,] *v' r2c' r2
eigenvalues = poles of χ
eigenvectors = oscillator strengths
Kohn-Sham excitation energies
4-points Hartree+xc kernel
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DP license:Scientific Software Open Source
Academic for Free LicenseAcademic, non-commercial, non-military purposes:• freedom to: use, copy, modify and redistribute
(like GPL)• open source (like GPL)• cost: for free (in the sense gratis, royalty free)• scientific behaviour: request of citationCommercial purposes:• excluded by this license, but allowed under
separate negotiation and different license
http://www.dp-code.org/download http://www.dp-code.org/license
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Conclusions• TDDFT is a valid tool of Condensed Matter Theoretical Physics to
calculate from first principles excited-state properties;• The agreement with the experiment is good, but the choice of the
right xc-approximation with respect to the given excited state property is crucial:– RPA with LF is able to reproduce EELS spectra at q=0;
– TDLDA improves upon RPA on EELS (and also IXSS, CIXS) spectra at high q;
– TDLDA seems also to improve upon RPA on optical spectra in finite systems;
– More refined kernels (LRC, MT) are required to reproduce optical spectra in solids, especially in presence of strong excitonic effects and bound excitons.
• Perspectives:– Improve the algorithms, simplify the orbital expressions of the kernel, find
a density-functional dependent kernel.